- Research article
- Open Access
Human neutrophil migration and activation by BJcuL, a galactose binding lectin purified from Bothrops jararacussu venom
© Elifio-Esposito et al; licensee BioMed Central Ltd. 2011
Received: 27 October 2010
Accepted: 25 January 2011
Published: 25 January 2011
Neutrophil migration to an inflamed site constitutes the first line of the innate immune response against invading microorganisms. Given the crucial role of endogenous lectins in neutrophil mobilization and activation, lectins from exogenous sources have often been considered as putative modulators of leukocyte function. Lectins purified from snake venom have been described as galactoside ligands that induce erythrocyte agglutination and platelet aggregation. This study evaluated human neutrophil migration and activation by C-type lectin BJcuL purified from Bothrops jararacussu venom.
Utilizing fluorescence microscopy, we observed that biotinylated-BJcuL was evenly distributed on the neutrophil surface, selectively inhibited by D-galactose. Lectin was able to induce modification in the neutrophil morphology in a spherical shape for a polarized observed by optical microscopy and exposure to BJcuL in a Boyden chamber assay resulted in cell migration. After 30 minutes of incubation with BJcuL we found enhanced neutrophil functions, such as respiratory burst, zymozan phagocytosis and an increase in lissosomal volume. In addition, BJcuL delays late apoptosis neutrophils.
These results demonstrate that BJcuL can be implicated in a wide variety of immunological functions including first-line defense against pathogens, cell trafficking and induction of the innate immune response since lectin was capable of inducing potent neutrophil activation.
Neutrophils are key players in the innate immune response and their recruitment from the microvasculature to inflammation sites includes rolling, firm adhesion, and transmigration through the vessel wall . Neutrophil activation leads to directed migration with changes in cell morphology from rounded cells covered with microvilli to elongated ruffled cells [2, 3]. Neutrophils exert their bactericidal activity at the inflammatory site through recognition and phagocytosis of the infectious agent, generation of toxic oxygen derivatives, and release of microbicidal molecules from their specialized lysosomes and granules . This sequential process relies on neutrophil interaction with chemoattractants, cytokines and other inflammatory mediators .
Viperid and elapid snake venoms contain complex mixtures of pharmacologically active molecules, including enzymes and proteins without enzymatic activity, such as C-type lectins. Based on their structural and functional properties snake venom C-type lectins have been classified as true C-type lectins, which contain a carbohydrate recognition domain (CRD) and bind to a specific sugar molecule, and the C-type lectin-like domain proteins (CTLDs) with CRD-related non-carbohydrate-binding domains that do not bind to a sugar moiety [6, 7], but act as factor IX/X-binding proteins and those interacting with platelet receptors .
Bothrops jararacussu venom lectin (BJcuL) is typically a C-type lectin with specificity to galactose units  and is unable to promote human platelets aggregation or even disrupt aggregation induced by ADP or thrombin . In murine models it is capable of producing edema, increasing vascular permeability  and directly inducing cellular infiltration in endothelial cells of post capillary venules, creating an adhesive surface for leukocyte rolling . All of these reports indicate that BJcuL may be involved in the inflammatory process and the activation of immune responses; however, these immunological properties and biological activities are still unclear. It is currently recognized that the role of neutrophils and macrophages is not restricted to phagocytosis and pathogen killing, but that these cells are essential for immunity and for building and modulating the innate response. In this study we analyzed the ability of BJcuL to induce neutrophil activation observed by cell polarization, migration, and adhesion, as well as increase in phagocytosis, generation of respiratory burst, increase of the lysosomes volume, and inhibition of spontaneous apoptosis.
BJcuL recognizes specific glycoligands on the human neutrophil surface
BJcuL induces polarization of human neutrophils
BJcuL induces neutrophil migration in vitro
BJcuL enhances neutrophil adhesion to fibronectin and matrigel
Increase of human neutrophil killing and phagocytosis induced by BJcuL
Uptake of neutral red by human neutrophils - Neutral red is a vital stain that accumulates in neutrophils and monocyte lysosomes  depending on the level of cell activation . Results show that stimulated cells present increased lysosomal volume when compared to non-stimulated cells (incubated with PBS only). BJcuL (2.5 μg/ml) increased lysosomal content in neutrophils (Figure 5B), complementing the observed phagocytic activity.
Superoxide production - The superoxide anion production was also evaluated in human neutrophils after incubation with BJcuL and positive controls (as described above), and negative control (PBS). The results demonstrated that BJcuL induced superoxide release as well as its positive controls (Figure 5C).
Anti-apoptotic effect of BJcuL on human neutrophils
Neutrophils are key cells in the innate immune system and can be activated by a variety of endogenous and exogenous substances. It has been shown that BJcuL promotes neutrophil recruitment in vivo, as it induces rolling and adherence of leukocytes acting directly on endothelial cells of post-capillary venules . We found that BJcuL interacted with glycoligands on the neutrophil surface and that D-galactose treatment strongly abrogated lectin-cell interaction as well as cell polarization and migration. Protein-carbohydrate interactions occur in a number of processes in leukocytes [14, 15] and are believed to serve as major signals for the release of pro-inflammatory mediators such as cytokines, nitric oxide, leukotrienes, and platelet activator factor .
In vivo neutrophil migration in response to an inflammatory stimulus is a crucial event mediated by direct or indirect mechanisms. The latter involve cytokines and other chemoattractants released from mast cells, macrophages and endothelial cells, after antigen recognition [17–19]. The intraperitoneal injection of BJcuL caused significant neutrophil recruitment into the peritoneal cavity of mice (data not shown) and under in vitro conditions BJcuL induced significant cell chemotaxis, modulating neutrophil migration by a direct mechanism that is inhibited by a specific carbohydrate. Neutrophil recruitment requires adherence to the luminal surface of vascular endothelium and thus changes the spherical cell morphology to a morphologically polarized cell that is efficient in vector migration . Neutrophils stimulated by BJcuL respond promptly, presenting morphological changes that are typical of stimulated migrating cells. An intense increase in adhesion was also observed in wells coated with ECM proteins, particularly fibronectin, indicating that activation by lectin may promote the up-regulation of specific adhesion molecules, such as β-1 integrins, a family of membrane receptors devoted to cell adhesion to the extracellular matrix . Integrins, in particular, have a central role in the adhesion-dependent activation for adhesion, transmigration and respiratory burst, in a rapid and reversible manner.
The capacity to stimulate oxidative burst has been previously described for other lectins that, acting directly or in concert with other mediators, could trigger or modulate neutrophil activation [21, 22]. As a typical chemoattractant, BJcuL induced a rapid and expressive alteration of neutrophil ability in superoxide production and phagocytosis. We also observed that BJcuL inhibited late apoptosis in activated neutrophils until 24 hrs, but this effect seemed to be reversible once neutrophil apoptosis was gradually increased during the 24 hr period. BJcuL seemed to induce neutrophil activation and increase the life span of these cells, the time necessary for their biological function. Neutrophils undergoing apoptosis lose function and are subsequently recognized and engulfed by local macrophages, a process that is central to successful resolution of inflammation . A number of factors, including cytokines, chemical mediators, and bacterial products, such as LPS, have been shown to prolong functional lifespan of neutrophils by causing cellular activation [24, 25]. Stimulation of human neutrophils with TLR agonists  results in CXCL-8 production, up-regulation of CD11b, down-regulation of L-selectin, delayed apoptosis, enhanced phagocytosis and enhanced FMLP-induced superoxide release [27, 28]. The lectin-glycoligand receptors on the neutrophil surface recognized by BJcuL are still unknown, but it is clear that this interaction induces several biological responses, thus suggesting that lectin may be a powerful pro-inflammatory molecule.
In summary, the present study showed that BJcuL can recognize glycoligands on the neutrophil surface, and can promote in vitro polarization, migration and adhesion to extracellular matrix proteins. Lectin also induced neutrophil functional activation observed by phagocytic uptake, superoxide production, and delay in cell apoptosis. The effects observed by BJcuL seem to be mediated by cell surface D-galactose moieties. Understanding the intracellular mechanisms that induce neutrophil migration and activation by BJcuL is crucial for future investigation of therapeutic strategies.
Lectin Purification and Biotinylation
B. jararacussu lectin (BJcuL) was purified as described by Elifio-Esposito and col. (2007) . BJcuL biotinylation with sulfo-NHS-LC-biotin (Pierce) was performed according to the manufacturer's recommendations.
Human Neutrophil Isolation
Heparinized human blood from healthy volunteers was layered on a density gradient using Monopoly resolving medium (ICN Pharmaceuticals, Costa Mesa, CA, USA) and centrifuged at 400 × g for 30 min. Resulting preparations were 98% pure, and more than 95% of the neutrophils were viable as measured by trypan blue.
Localization of the lectin glycoligands on human neutrophil surface
Neutrophils (106 cells/ml) were placed on coverslips coated with Biobond (EM Science, Fort Washington, PA, USA), fixed with 2% formaldehyde at room temperature (RT) for 20 min and incubated with biotinylated BJcuL (10 μg/ml) at 37°C for 1 hr. After washing in PBS, the cells were incubated with streptavidin-FITC (GibcoBRL) for 30 min. Cell was mounted in histological slides with Fluormount-G. In some experiments, the lectin was pre-incubated with 2 mM D-galactose (Gal) or N-acetylglucosamine (GlcNAc).
Human neutrophils were plated at 106 cells/ml and were incubated with BJcuL (2.5 μg/ml), fMLP (10-6 M/well) or RPMI alone for 45 min at 37°C. In some experiments, before contact with neutrophils, the attractants were incubated for 45 min at RT with Gal or GlcNAc (2 mM). The proportion of neutrophil polarization was determined by a polarized and non-polarized cell count in a Neubauer chamber.
Human Neutrophil migration assay
Neutrophil migration was evaluated in a 48-well Boyden microchamber (Neuroprobe, USA) by which the top and bottom wells were separated with PVP-free polycarbonate filters (5-μm pore size, Nucleopore, USA). For chemotaxis induction BJcuL (2.5 μg/well), pre-incubated or not with Gal or GlcNAc (2 mM), or RPMI alone was added to the bottom wells, whereas the neutrophil suspension (1x106 cells/ml) was placed in the top wells. Following an incubation time of 40 min, at 37°C and 5% CO2, the cells were stained with HEMA 3 and the number of cells migrating through polycarbonate filters was counted in five fields for each condition, assayed in triplicate.
The adhesion assays were carried out in 96-well microplates. Each well was previously coated with fibronectin or matrigel (250 ng/ml) diluted in 0.2 M sodium carbonate pH 9,6 for 16 hrs at 4°C. The isolated neutrophils (1 × 104/ml) were added in solutions of BJcuL (2.5 μg/ml) or only RPMI. After a 4 hr incubation at 37°C and 5% CO2, the non-adherent cells were removed by three successive washes with PBS. The adhered cell layer was fixed for 10 min with methanol, washed with PBS and then stained with 0.2% crystal violet for 5 min. After staining, the wells were repeatedly washed with PBS. The cells were lysed with sodium citrate 100 mM in ethanol and the absorbance was measured at 550 nm (Microplate Reader Benchmark - Bio-Rad Laboratories, San Francisco, CA, USA). Unspecific adhesion was evaluated in the absence of extracellular matrix protein.
Neutrophil suspension (1 × 104/ml) was added to the wells of a 96-well microplate and incubated with BJcuL (2.5 μg/ml), PMA (1 μg/ml) or CXCL8 (2 μg/ml) (Sigma Chemical Company) diluted in a solution containing neutral-red dye and zymosan (2.3 × 108 particles/ml) for 30 min at 37°C. After incubation, cells were fixed with Baker's formaldehyde-calcium for 30 min and then washed twice by centrifugation (453 × g for 5 min). The neutral-red stain incorporated by the cells was solubilized by acidified ethanol in each well. After 30 min, the absorbance at 550 nm was detected.
Uptake of neutral red by activated neutrophils
The uptake of the cationic dye, neutral red, which concentrates in cell lysosomes , was used to assess neutrophil volume of the lysosomal system. Neutrophil suspension (1 × 104/ml) was added to the wells in a 96-well microplate in the presence of BJcuL (2.5 μg/ml), PMA (1 μg/ml) or CXCL8 (2 μg/ml) and 3% neutral red in PBS for 30 min at 37°C. Cells were then washed twice with PBS by centrifugation (453 × g for 5 min). Neutral red was solubilized by 30 min incubation with acidified ethanol solution at RT and the absorbance was read at 550 nm.
Superoxide production was estimated by nitro-blue tetrazolium (NBT) reduction assay. Neutrophils (1 × 104 cells/ml) were incubated for 30 min at 37°C in the presence of BJcuL (2.5 μg/ml), PMA (1 μg/ml) or CXCL8 (2 μg/ml) and 0.1% NBT (Sigma Chemical Company). The reaction was stopped by the addition of acetic acid. The mixture was then centrifuged for 30 sec at 2500 × g. Reduction of NBT results in the formation of blue formazan, which was detected at 560 nm.
Neutrophils (1 × 106/ml) were incubated for 12, 18 and 24 hrs at 37°C with BJcuL (2.5 μg/ml) and stained with propidium iodide and FITC-labeled Annexin-V, according to manufacturer's instructions.
All results are reported as means ± Standard Deviation (SD). Analysis of variance (ANOVA) was used to compare means between treatment and control groups. Student's t-test was used to determine if the control assay was significantly different when compared to the lectin assay. P-values of 0.05 or less were regarded as statistically significance.
We thank the Instituto Butantan/SP for providing B. jararacussu venom. This research was supported by grants from CNPq and PIBIC/PUCPR.
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